US3323978A - Artificial textile fibres and their production - Google Patents

Artificial textile fibres and their production Download PDF

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Publication number
US3323978A
US3323978A US27920463A US3323978A US 3323978 A US3323978 A US 3323978A US 27920463 A US27920463 A US 27920463A US 3323978 A US3323978 A US 3323978A
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Prior art keywords
polymer
hydrophilic
fibres
hydrophobic
film
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Rasmussen Ole-Bendt
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ConocoPhillips Co
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ConocoPhillips Co
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    • DTEXTILES; PAPER
    • D01NATURAL OR ARTIFICIAL THREADS OR FIBRES; SPINNING
    • D01DMECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00Formation of filaments, threads, or the like
    • D01D5/42Formation of filaments, threads, or the like by cutting films into narrow ribbons or filaments or by fibrillation of films or filaments
    • D01D5/423Formation of filaments, threads, or the like by cutting films into narrow ribbons or filaments or by fibrillation of films or filaments by fibrillation of films or filaments
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/08Fibrillating cellular materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/47Processes of splitting film, webs or sheets
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/2964Artificial fiber or filament
    • Y10T428/2967Synthetic resin or polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2973Particular cross section
    • Y10T428/2978Surface characteristic

Description

June 6, 1967 oLE-BENDT RASMUSSEN 3,323,978

ARTIFICIAL TEXTILE FIBRES AND THER PRODUCTION Filed May 9. 1965 Ona/,fling :47m @fre/ching a/ increased lempefaare /0 f". 3 "III.. 'ff-,

'lll I United States Patent O 3,323,978 AR'HFiClAL TEXTILE HERES AND THEIR PRDUCTION @le-Berndt Rasmussen, Birkerorl, Denmark, assigner to Phillips Petroleum Company, Bartlesville, Ghia., a corporation of Deiaware Filed May 9, 1963, Ser. No. 279,204 7 Claims. (Cl. MSL-159) The invention relates to artificial textile fibres having a hydrophilic surface, and to methods for their production from an oriented film material.

It is an object of the invention to provide for artificial textile fibres combining the advantages of the hydrophobic synthetic fibres with the capability of the hydrophilic fibres, eg. several natural fibres, to absorb clamminess of the body, t-o lresist electrostatic charging, and to be easily dyed. The advantages as referred to here of the hydrophobic synthetic fibres are particularly their ability of resisting shrinkage on washing in hot water, and their independence upon the humidity of the surroundings in `regard of strength and elasticity.

It has been suggested to combine the said properties by providing hydrophobic fibres with a coating of a hydrophilic polymer substance, for example by coating nylon fibres with polyvinyl alcohol, but a satisfying connection between the two substances could not be obtained so that the coating was too easily worn off.

In experiments preceding the present invention use has been made of a splitting process in order to provide for a relatively hydrophilic coating upon fibres of certain selected crystalline polymers, for example polycaprolactam. In these experiments, at first a film of the polymer was produced which was then oriented, after which the polymer was swelled and, finally, a splitting was carried out, for example by means of ultra-sound, while the polymer was still under the influence of the swelling agent. Since substances of the nature of polycaprolactam consist of crystalline and amorphous parts, and since it is mainly the amorphous parts that are attacked by the swelling agent, the splitting occurs mainly in the latter parts. Thereby, the surface of the fibres produced by the splitting becomes substantially more amorphous than do the remaining parts of the fibre material, and since polycaprolactam is substantially more hydrophilic in amorphous form than in crystalline form, fibres are obtained having in a manner of speaking a hydrophilic coating intimately connected with a relatively hydrophobic core. This method of producing a predominantly hydrophilic surface on predominantly hydrophobic libres, however, can be used only in substances, such as polycaprolactam, which are intermediates between the hydrophilic and the hydrophobic polymers, and which are having incidentally a partly crystalline structure.

The fibres of the present invention a-re of the type called splitfibres, i.e. individual fibres or a network of fibres produced by subjecting an oriented organic synthetic polymer material to a splitting process.

The fibres of the invention are characterized in that the material of the fibres is of a two-phase structure with parts of an oriented distinctly hydrophobic polymer alternating with parts yof another polymer of distinctly hydrophilic, or latently hydrophilic, character, the fibres having a predominantly hydrophobic core and an ac- 3,323,978 Patented June 6, 1967 ice cumulation of the distinctly hydrophilic, or latently hydrophilic, polymer in spots on the surface.

The said two-phase structure can be obtained, for example, by producing a solution of the two polymers and casting a film from this solution, whereby during the drying first one polymer is precipitated, forming a gel structure in the solution, after which the other polymer is precipitated by the continued drying.

Other manners of obtaining the two-phase structure is by extruding a mixture of the two polymers, or by casting a film from a mixture of suspensions of the two polymers.

A preferred method of producing the fibres of the invention is characterized in that a lm material is first produced, consisting of a synthetic polymer material comprising a distinctly hydrophobic component and a distinctly hydrophilic component, if desired with latent hydrophility, after which the said film material is treated with a strong-acting swelling agent for the distinctly hydrophilic component, the swelled product being subsequently split in known manner into individual fibres or into a coherent network of fibres and, if the hydrophility is latent, subjected to a treatment to develop the hydrophility.

It has been found that after strong orienting, the film material of the said kind comprising a distinctly hydrophobic and a distinctly hydrophilic component, forms a fibrillar two-phase microstructure. By swelling, the material of the hydrophilic fibrils is weakened, and the surfaces of the splits resulting from the subsequent splitting process will therefore mainly be in the hydrophilic substance so that the fibres will have an accumulation of hydrophilic substance at the surfaces. In this manner a very desirable combination is obtained of the said advantages of the hydrophilic and of the hydrophobic fibres, respectively.

As stated, -orienting and splitting is carried out by well known methods. As regards the splitting process it will generally be advantageous -to start with producing microscopic splits by incorporating in the material particles which are made to expand. If desired, this can take place before the treatment with the swelling agent. The resulting loosening of the structure facilitates the subsequent mechanical splitting. Advantageously, the splitting is started in known manner by sandwiching the film material between two rubber plates or endless rubber belts and stretching the latter at a right angle to the direction of orientation of the material, continuing the splitting treatmen-t, for example, by ultrasonic means in a bath of liquid.

Often, it will be advantageous to make the said fibrillar two-phase structu-re more pronounced by means of a heat treatment before the swelling.

In an embodiment of carrying out the present invention, the film material is produced by `mixing a hydrophobic synthetic polymer with a smaller amount of a hydrophilic polymer, and adding a graft or block polymer which on account of it surface-active effect improves and strengthens the connection between the said two components.

Examples of polymers of distinct hydrophility are polyoxyethylene, polyvinyl alcohol, and co-polymerisates on the basis of acrylic .acid or methacrylic acid.

As stated, however, the hydrophility may be latent, a component being used which is not in itself particularly hydrophilic, but which can be transformed so as to become distinctly hydrophilic Without the hydrophobic substance being substantially attacked simultaneously, the said transformation then being made after the splitting has been carried out. The advantage of this is that the mixing process and the swelling are both facilitated. Briefly stated, the hydrophilic groups are masked during the said processes. Among others, esters of polyacids, such as polyacrylates or polymethacrylates, or esters or acetals of polyalcohols, such as polyvinyl esters, polyallyl esters, and polyvinylacetal can be used, the swelling being carried out by means of non-aqueous liquid being able to easily penetrate the hydrophobic component, the hydrophility being developed by total or partial hydrolysis or alcoholysis after the splitting. It will often be advantageous according to the invention -to proceed in the manner that the film material is produced from a hydrophobic synthetic polymer and a graft or block polymer containing groups which give or can be made to give the latter polymer a distinct hydrophility.

The distinctly hydrophobic polymer component can advantageously be polyethylene with a high specific weight, crystalline polypropylene or polyvinylidene chloride, including co-polymerisates of the latter substance, but besides any distinctly hydrophobic synthetic polymer can be used. The said three polymers are all very cheap, especially polyethylene, and thus the present invention brings a solution of the problem how to produce refined textile fibres from these compounds by cheap methods and means.

As known, polyvinylidene chloride has the specific advantage of being self-extinguishing, but has not hitherto been used to any greater extent for proper textile purposes owing to the failing capacity of absorbing the clamminess of the body. As known, polypropylene has a particularly good tensile strength `and also good textile properties in other respects. However, also the use of this substance for textile purposes has hitherto been inhibited owing to the failing capacity of adsorbing the clamminess of the body.

As regards the graft or block polymer to be used, the skilled artisan can easily make his choice on the basis of the comprehensive scientific literature which exists concerning the production and properties of the said substances. Generally, substances of the said kind are chosen, one component of which is identical with or closely related to the hydrophobic component which is used. In case the film to be split is produced using a graft or block polymer, a cheap substance of the said kind is preferably chosen, and it should be noted that graft polymerisates based upon polyproylene are both cheap and in other ways well suited for the purpose.

Example A 0.06 mm. thick film is cast from a 20% solution in hot xylene of high density polyethylene and polyvinyl acetate in the proportions of 3:1 by`weight. On drying the solution, the polyethylene first precipitates in gel form in the solution containing dissolved polyvinyl acetate. The dry film, being very fragile at room temperature, is oriented by stretching at 110 C. in the ratio of 10:1, thus acquiring a high tensile strength and ability to split.

The film is placed in an acetone bath for 1 2 minutes, causing the polyvinyl acetate, but not the polyethylene, -to swell.

After drying the surfaces, the swelled film is split up to a coherent network of fibres by sandwiching the film between a pair of continuous rubber belts which are being kept together by means of water pressure at 5 atmospheres. By gradually laterally distending the travelling rubber belts enclosing the oriented film, the splitting of the lat-ter is accomplished.

In order to keep the film -in the swelled state during the splitting, a paste of pulverized silica gel in acetone is applied to the rubber belts.

Finally, the network of fibres is passed through a hot acid-bath in order to develop the hydrophility of the fibre surfaces by partly hydrolyzing the spots of polyvinyl acetate to polyvinyl alcohol.

Since the hydrophilic parts are easily dyed, contrary to the hydrophobic parts, a dyeing process can be used for proving the two-phase structure of the fibres, and the accumulation of the hydrophilic component on the surface of the individual fibres. A direct cotton dye as normally used is suitable for the said dyeing.

The invention is further illustrated by the accompanying drawing in which FIG. 1 is a fiow sheet illustrating a method of producing the fibres,

FIG. 2 is an enlarged section through part of a stretched film, and

FIG. 3 is an enlarged part of an individual fibre.

In FIG. 2, an arrow 5 represents the stretching direction. The film consists of a hydrophobic polymer 6 having embedded therein oblong parts 7 of a hydrophobic polymer. Upon mechanical splitting, the clefts proceed mainly through the hydrophilic parts as illustrated by dashed lines S to give fibres as the one illustrated in FIG. 3 showing spots 9 of the hydrophilic polymer on the surface of a mainly hydrophobic core 10.

I claim:

1. A fibrous product of organic synthetic material comprising a two-phase structure including a continuous core portion of an oriented, normally crystalline, predominantly hydrophobic polymer, and a discontinuous surface portion of a different distinctly hydrophilic polymer.

2. A fibrous product of organic synthetic material cornprising a plurality of fibres in a coherent network in which each fibre element has a two-phase structure including a continuous core portion of an oriented, normally crystalline, predominantly hydrophobic polymer selected from the group consisting of polyethylene, polypropylene and polyvinylidene chloride, and a discontinuous surface port-ion of a different distinctly hydrophilic polymer selected from the group consisting of polyvinyl alcohol, polyoxyethylene, co'polymerizates of acrylic acid and of methacrylic acid, and hydrolyzed polymers selected from the group consisting of esters of polyacids, esters of polyalcohols and `acetals of polyalcohols.

3. A method of making a synthetic fibrous product which comprises blending a normally crystalline, predominantly hydrophobic polymer with a smaller amount of a different polymer which is distinctly hydrophilic or potentially hydrophilic on hydrolysis, forming the resulting blend into a film, stretching said film so as to orient uniaxially the crystalline polymer component, treating the oriented film with a swelling agent for said hydrophilic polymer, and splitting said film into a fibrous structure.

4. The method of claim 3 wherein said fibrous structure is treated with a hydrolysis agent to hydrolyze any potentially hydrophilic polymer present at the surface of the fibres.

5. A method of making a synthetic fibrous product which comprises blending a normally crystalline, predominantly hydrophobic polymer selected from the group consisting of polyethylene, polypropylene and polyvinylidene chloride with a smaller amount of a different polymer which is distinctly hydrophilic or potentially hydrophilic on hydrolysis, selected from the group consisting of polyvinyl alcohol, polyoxyethylene, copolymerizates of acrylic acid and of methacrylic acid, and hydrolyzed polymers selected from the group consisting of esters of polyacids, esters of polyalcohols and acetals of polyalcohols, forming the resulting blend yinto a lm, stretching said film so as to orient uniaxially the crystalline polymer component, treating the oriented lm with a swelling agent for said hydrophilic polymer, and splitting said film into a fibrous structure.

5 6 6. Method according7 to claim 3 wherein the lm ma- References Cited terial is produced by mixing a hydrophobic synthetic poly- UNITED STATES PATENTS mer with a smaller proportion of a hydrophilic polymer, 2 700 657 1/1955 Look et al 18 54 X and a graft or block polymer is added which on account 954387 17o/1960 Rasmussen' 18 54 X of its surface-active elect brings about the connection be- 5 3,097,991

7/1963 Miller et al 18*54 X tween said two components.

7. Method'according to claim 3 wherein the film ma- FOREIGN PTENTS terial is produced from a hydrophobic synthetic polymer 211,133 12/ 1955 AllSalland a graft or block polymer containing groups which are EARL M BERG-ERT, primary Examinelg giving or can be made to give the latter polymer a dis- A 1 SMEDEROVAC, R A FLORES, tinct hydrophility. Assistant Examiners.

Claims (1)

  1. 2. A FIBROUS PRODUCT OF ORGANIC SYNTHETIC MATERIAL COMPRISING A PLURALITY OF FIBRES IN A COHERENT NETWORK IN WHICH EACH FIBRE ELEMENT HAS A TWO-PHASE STRUCTURE INCLUDING A CONTINUOUS CORE PORTION OF AN ORIENTED, NORMALLY CRYSTALLINE, PREDOMINANTLY HYDROPHOBIC POLYMER SELECTED FROM THE GROUP CONSISTING OF POLYETHYLENE, POLYPROPYLENE AND POLYVINYLIDENE CHLORIDE, AND A DISCONTINUOS SURFACE PORTION OF A DIFFERENT DISTINCTLY HYDROPHILIC POLYMER SELECTED FROM THE GROUP CONSISTING OF POLYVINYL ALCOHOL, POLYOXYETHYLENE, COPOLYMERIZATES OF ACRYLIC ACID AND OF METHACRYLIC ACID, AND HYDROLYZED POLYMERS SELECTED FROM THE GROUP CONSISTING OF ESTERS OF POLYACIDS, ESTERS OF POLYALCOHOLS AND ACETALS OF POLYALCOHOLS.
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Cited By (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3398441A (en) * 1965-12-03 1968-08-27 Asahi Chemical Ind Method of producing crimped fibrous material
US3407249A (en) * 1966-01-25 1968-10-22 American Cyanamid Co Porous, extensively fibrillated polytetrafluoroethylene and method of preparing same
US3443002A (en) * 1966-10-26 1969-05-06 Asahi Chemical Ind Process for producing crimped filaments
US3520762A (en) * 1967-03-24 1970-07-14 Asahi Chemical Ind Pile fabric
US3549734A (en) * 1967-06-27 1970-12-22 Takeshi Yasuda Method of forming microfibers
US3673291A (en) * 1967-12-28 1972-06-27 Rasmussen O B Method for the production of synthetic sheet materials
US3957936A (en) * 1971-07-22 1976-05-18 Raduner & Co., Ag High temperature process for modifying thermoplastic filamentous material
US4814131A (en) * 1987-07-02 1989-03-21 Atlas Sheldon M Process for producing a shaped article, such as fiber composed of a hydrophobic polymer and a hydrophilic polymer
US5700872A (en) * 1996-12-31 1997-12-23 Kimberly Clark Worlwide, Inc. Process for making blends of polyolefin and poly(ethylene oxide)
US5759926A (en) * 1995-06-07 1998-06-02 Kimberly-Clark Worldwide, Inc. Fine denier fibers and fabrics made therefrom
US5912076A (en) * 1996-12-31 1999-06-15 Kimberly-Clark Worldwide, Inc. Blends of polyethylene and peo having inverse phase morphology and method of making the blends
US5916969A (en) * 1996-11-22 1999-06-29 Kimberly-Clark Corporation Article and composition of matter made from polyolefins and PEO blend and method of making the same
US6063866A (en) * 1996-12-31 2000-05-16 Kimberly-Clark Worldwide, Inc. Blends of polyolefin and poly(ethylene oxide) and process for making the blends
US6071451A (en) * 1997-12-31 2000-06-06 Kimberly-Clark Worldwide, Inc. Process for making a nonwoven, porous fabric from polymer composite materials
US6090472A (en) * 1997-12-31 2000-07-18 Kimberly-Clark Worldwide, Inc. Nonwoven, porous fabric produced from polymer composite materials
US6100330A (en) * 1996-12-31 2000-08-08 Kimberly-Clark Worldwide, Inc. Water-degradable film of monomer grafted to polyolefin and poly(ethylene oxide)
US6107405A (en) * 1996-10-18 2000-08-22 Kimberly Clark Corporation Method of making grafted polyolefin compositions
US6111014A (en) * 1996-12-31 2000-08-29 Kimberly-Clark Worldwide, Inc. Film of monomer-grafted polyolefin and poly(ethylene oxide)
US6117947A (en) * 1997-12-31 2000-09-12 Kimberly-Clark Worldwide, Inc. Method of modifying poly(ethylene oxide)
US6153700A (en) * 1996-12-31 2000-11-28 Kimberly-Clark Worldwide, Inc. Water-degradable flushable film of polyolefin and poly(ethylene oxide) and personal care article therewith
US6255386B1 (en) 1996-12-31 2001-07-03 Kimberly-Clark Worldwide, Inc. Blends of polyolefin and poly(ethylene oxide) and process for making the blends
US6261674B1 (en) 1998-12-28 2001-07-17 Kimberly-Clark Worldwide, Inc. Breathable microlayer polymer film and articles including same
US6297326B1 (en) 1996-10-18 2001-10-02 Kimberly-Clark Corporation Grafted polyolefin compositions
US6350518B1 (en) 1998-06-01 2002-02-26 Kimberly-Clark Worldwide, Inc. Methods of making blend compositions of an unmodified poly vinyl alcohol and a thermoplastic elastomer
US6372850B2 (en) 1997-12-31 2002-04-16 Kimberly-Clark Worldwide, Inc. Melt processable poly (ethylene oxide) fibers
US6403706B1 (en) 2000-12-28 2002-06-11 Kimberly-Clark Worldwide, Inc. Methods of making polymer/dispersed modifier compositions
US6495080B1 (en) 1997-10-03 2002-12-17 Kimberly-Clark Worldwide, Inc. Methods for making water-sensitive compositions for improved processability and fibers including same
US6515075B1 (en) 2001-07-12 2003-02-04 Kimberly-Clark Worldwide, Inc. Films, fibers and articles of chemically modified polyethylene oxide compositions with improved environmental stability and method of making same
US20030078555A1 (en) * 1998-12-29 2003-04-24 John Kerins Body-activated adhesive compositions, films, personal care articles and pantiliners
US6576576B1 (en) 1999-12-29 2003-06-10 Kimberly-Clark Worldwide, Inc. Multicomponent fibers
US6607819B2 (en) 2000-12-28 2003-08-19 Kimberly-Clark Worldwide, Inc. Polymer/dispersed modifier compositions
US6610793B1 (en) 2000-05-26 2003-08-26 Kimberly-Clark Worldwide, Inc. Modified poly(ethylene oxide), method of making same and articles using same
US6624100B1 (en) 1995-11-30 2003-09-23 Kimberly-Clark Worldwide, Inc. Microfiber nonwoven web laminates
US6790519B1 (en) 2000-05-26 2004-09-14 Kimberly-Clark Worldwide, Inc. Moisture-induced poly(ethylene oxide) gel, method of making same and articles using same

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US2700657A (en) * 1951-11-13 1955-01-25 Dow Chemical Co Melt-spinnable, fiber forming blend of polystyrene and specific styrene-acrylonitrile interpolymers
US2954587A (en) * 1954-05-29 1960-10-04 Rasmussen Ole-Bendt Method of producing fibrous materials
US3097991A (en) * 1957-06-10 1963-07-16 Union Carbide Corp Synthetic fibrous products

Patent Citations (3)

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Publication number Priority date Publication date Assignee Title
US2700657A (en) * 1951-11-13 1955-01-25 Dow Chemical Co Melt-spinnable, fiber forming blend of polystyrene and specific styrene-acrylonitrile interpolymers
US2954587A (en) * 1954-05-29 1960-10-04 Rasmussen Ole-Bendt Method of producing fibrous materials
US3097991A (en) * 1957-06-10 1963-07-16 Union Carbide Corp Synthetic fibrous products

Cited By (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3398441A (en) * 1965-12-03 1968-08-27 Asahi Chemical Ind Method of producing crimped fibrous material
US3407249A (en) * 1966-01-25 1968-10-22 American Cyanamid Co Porous, extensively fibrillated polytetrafluoroethylene and method of preparing same
US3443002A (en) * 1966-10-26 1969-05-06 Asahi Chemical Ind Process for producing crimped filaments
US3520762A (en) * 1967-03-24 1970-07-14 Asahi Chemical Ind Pile fabric
US3549734A (en) * 1967-06-27 1970-12-22 Takeshi Yasuda Method of forming microfibers
US3673291A (en) * 1967-12-28 1972-06-27 Rasmussen O B Method for the production of synthetic sheet materials
US3957936A (en) * 1971-07-22 1976-05-18 Raduner & Co., Ag High temperature process for modifying thermoplastic filamentous material
US4814131A (en) * 1987-07-02 1989-03-21 Atlas Sheldon M Process for producing a shaped article, such as fiber composed of a hydrophobic polymer and a hydrophilic polymer
US5759926A (en) * 1995-06-07 1998-06-02 Kimberly-Clark Worldwide, Inc. Fine denier fibers and fabrics made therefrom
US6624100B1 (en) 1995-11-30 2003-09-23 Kimberly-Clark Worldwide, Inc. Microfiber nonwoven web laminates
US6107405A (en) * 1996-10-18 2000-08-22 Kimberly Clark Corporation Method of making grafted polyolefin compositions
US6297326B1 (en) 1996-10-18 2001-10-02 Kimberly-Clark Corporation Grafted polyolefin compositions
US5916969A (en) * 1996-11-22 1999-06-29 Kimberly-Clark Corporation Article and composition of matter made from polyolefins and PEO blend and method of making the same
US6111014A (en) * 1996-12-31 2000-08-29 Kimberly-Clark Worldwide, Inc. Film of monomer-grafted polyolefin and poly(ethylene oxide)
US6359063B1 (en) 1996-12-31 2002-03-19 Kimberly-Clark Worldwide, Inc. Personal care article with layer of monomer-grafted polyolefin and PEO
US6362277B1 (en) 1996-12-31 2002-03-26 Kimberly-Clark Worldwide, Inc. Personal care article with layer of monomer-grafted polyolefin and unmodified PEO
US6100330A (en) * 1996-12-31 2000-08-08 Kimberly-Clark Worldwide, Inc. Water-degradable film of monomer grafted to polyolefin and poly(ethylene oxide)
US5807930A (en) * 1996-12-31 1998-09-15 Kimberly-Clark Worldwide, Inc. Process for making blends of polyolefin and poly(ethylene oxide)
US6063866A (en) * 1996-12-31 2000-05-16 Kimberly-Clark Worldwide, Inc. Blends of polyolefin and poly(ethylene oxide) and process for making the blends
US5700872A (en) * 1996-12-31 1997-12-23 Kimberly Clark Worlwide, Inc. Process for making blends of polyolefin and poly(ethylene oxide)
US6153700A (en) * 1996-12-31 2000-11-28 Kimberly-Clark Worldwide, Inc. Water-degradable flushable film of polyolefin and poly(ethylene oxide) and personal care article therewith
US6225406B1 (en) 1996-12-31 2001-05-01 Kimberly-Clark Worldwide, Inc. Reactive extrusion method of making inverse phase blends of poly(ethylene oxide) and polyolefin
US6255386B1 (en) 1996-12-31 2001-07-03 Kimberly-Clark Worldwide, Inc. Blends of polyolefin and poly(ethylene oxide) and process for making the blends
US5912076A (en) * 1996-12-31 1999-06-15 Kimberly-Clark Worldwide, Inc. Blends of polyethylene and peo having inverse phase morphology and method of making the blends
US6495080B1 (en) 1997-10-03 2002-12-17 Kimberly-Clark Worldwide, Inc. Methods for making water-sensitive compositions for improved processability and fibers including same
US6071451A (en) * 1997-12-31 2000-06-06 Kimberly-Clark Worldwide, Inc. Process for making a nonwoven, porous fabric from polymer composite materials
US6750163B2 (en) 1997-12-31 2004-06-15 Kimberly-Clark Worldwide, Inc. Melt processable poly (ethylene oxide) fibers
US6090472A (en) * 1997-12-31 2000-07-18 Kimberly-Clark Worldwide, Inc. Nonwoven, porous fabric produced from polymer composite materials
US6372850B2 (en) 1997-12-31 2002-04-16 Kimberly-Clark Worldwide, Inc. Melt processable poly (ethylene oxide) fibers
US6117947A (en) * 1997-12-31 2000-09-12 Kimberly-Clark Worldwide, Inc. Method of modifying poly(ethylene oxide)
US6350518B1 (en) 1998-06-01 2002-02-26 Kimberly-Clark Worldwide, Inc. Methods of making blend compositions of an unmodified poly vinyl alcohol and a thermoplastic elastomer
US6261674B1 (en) 1998-12-28 2001-07-17 Kimberly-Clark Worldwide, Inc. Breathable microlayer polymer film and articles including same
US20030078555A1 (en) * 1998-12-29 2003-04-24 John Kerins Body-activated adhesive compositions, films, personal care articles and pantiliners
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